On completing your regulatory documentation, our medical communications (med comms) specialists can engage with your trial data to communicate your findings to the wider scientific community, incorporating your key messages, successfully introducing your medicinal product to a welcoming market.

Our experienced med comms writers can help you with your product launch goals through strategic publication planning (whilst adhering to good publication planning practice 3 [GPP3] guidelines), and creation of a range of medical communications documents including:

  • Manuscripts (clinical studies, meta-analyses, reviews, surveillance studies)
  • Medical and scientific literature searches and reviews
  • Conference articles, reports, and transcripts
  • Advisory board meetings and reports
  • Summary of product characteristics
  • Journal/conference submissions
  • Patient information leaflets
  • Publication planning
  • Editorial support
  • Journal articles
  • White papers
  • Monographs
  • Abstracts
  • Posters

Get in touch to learn how we can help you!